Uptake of magnesium by suspension cultures of plant cells (Ipomoea sp.)

1977 ◽  
Vol 55 (9) ◽  
pp. 1143-1147 ◽  
Author(s):  
I. A. Veliky ◽  
D. Rose ◽  
M. W. Zink

The magnesium level required to support full growth in batch suspension cultures of an Ipomoea sp. (Morning Glory) cell line in 2% sucrose media was less than 0.3 mM. The uptake of magnesium increased with increasing magnesium in the medium, and with increasing pH at constant magnesium level. In medium containing 1.0 mM (24 mg/ℓ) magnesium, a culture kept at pH 4.7 absorbed 6 mg of magnesium in 150 h; the corresponding figure for a culture kept at pH 6.9 was 19 mg.Much of the excess magnesium taken up by cells grown at the 1.0 mM magnesium level at various controlled pH levels could be extracted by grinding the cells in distilled water. The data suggest that under conditions of high magnesium supply and high pH these cells absorb large amounts (i.e. several milligrams per gram dry cells) of magnesium in excess of their requirement for growth.

1975 ◽  
Vol 53 (4) ◽  
pp. 315-320 ◽  
Author(s):  
Dyson Rose ◽  
S. M. Martin

Studies on the growth of batch suspension cultures of a plant cell line, initiated from Ipomoea sp. root explants, at temperatures ranging from 15 to 34 °C are reported. Maximum growth of cultures of this cell line occurred between 25 and 32 °C, with temperature variations within this range having little effect on growth rates based on dry cell yields. Cultivation at 20 °C substantially reduced the growth rate. However, cells grown at 20 °C failed to grow on transfer to fresh medium at 20 °C. Thus cultivation at suboptimum temperatures is not a satisfactory method for routine maintenance of the suspension culture.


Planta Medica ◽  
2018 ◽  
Vol 84 (09/10) ◽  
pp. 743-748
Author(s):  
Suvi Häkkinen ◽  
Heli Nygren ◽  
Natalia Maiorova ◽  
Raisa Haavikko ◽  
Sami Alakurtti ◽  
...  

AbstractIn this study, three semisynthetic betulonic acid-based compounds, 20(29)-dihydrolup-2-en[2,3-d]isoxazol-28-oic acid, 1-betulonoylpyrrolidine, and lupa-2,20(29)-dieno[2,3-b]pyrazin-28-oic acid, were studied in biotransformation experiments using Nicotiana tabacum and Catharanthus roseus cell suspension cultures. Biotransformation was performed using cyclodextrin to aid dissolving poorly water-soluble substrates. Several new derivatives were found, consisting of oxidized and glycosylated (pentose- and hexose-conjugated) products.


1986 ◽  
Vol 18 (10) ◽  
pp. 157-157
Author(s):  
K E. U. Brodisch ◽  
G. K. Idema ◽  
P. Coubrough ◽  
W O. K. Grabow

Shellfish meat was seeded with polio and reoviruses, the SA11 simian rotavirus and two coliphages, VI and MS2, in order to study methods of virus recovery. An adsorption-elution-flocculation procedure had an efficiency of recovery of about 66% for poliovirus, but only 3% for reovirus, 1% for SA11 virus and 2% for the two coliphages. The poor efficiency of recovery of all viruses except poliovirus, may be due to inactivation by exposure to low and high pH levels which form part of the recovery procedure. In another procedure seeded shellfish meat was simply homogenized in distilled water and centrifuged. The supernatant was decontaminated with chloroform and directly analyzed. The efficiency of recovery of this procedure was only about 8% for poliovirus, but 44% for MS2 and 50% for VI phages. Chloroform treatment had an adverse effect on the phages, because the elimination of this step increased the efficiency of recovery to 50% for MS2 and 62% for VI. These results indicate that the phages do not adsorb tightly to the shellfish meat and can, therefore, readily be recovered. Enteric viruses, on the other hand, adsorb tightly to shellfish meat and special procedures are required to accomplish meaningful recovery. These findings suggest that different procedures should be used for the recovery of various viruses from shellfish meat.


Nature ◽  
1968 ◽  
Vol 220 (5167) ◽  
pp. 604-605 ◽  
Author(s):  
O. L. GAMBORG ◽  
T. A. G. LARUE

1976 ◽  
Vol 54 (11) ◽  
pp. 1264-1270 ◽  
Author(s):  
S. M. Martin ◽  
Dyson Rose

Suspension cultures of a plant cell line initiated from Ipomoea sp. root tissue were grown in defined medium at controlled pH levels of 4.8, 5.6, 6.4, and 7.1 with ammonium and nitrate as the nitrogen sources. Biomass yield was less at pH 4.8 and 7.1 than at the intermediate pH levels. At pH 7.1, this resulted from the inability of the culture to utilize nitrate. At pH 4.8, the cause of the low yield was not apparent but was probably related to a less efficient utilization of sucrose.The ability of the cells to utilize ammonium increased with increasing pH, with a possible maximum at pH 6.4. The ability to utilize nitrate decreased with increasing pH and was essentially zero at pH 7.1. At pH 4.8, ammonium was released into the medium during part of the growth cycle, indicating that the rate of nitrate reduction exceeded the rate of incorporation of the ammonium thus formed.Utilization of nitrate was not inhibited by the presence of ammonium.


2007 ◽  
Vol 25 (2) ◽  
pp. 109-115
Author(s):  
Wayne A. Mackay ◽  
Michael A. Arnold ◽  
Garry V. McDonald ◽  
Narendra Sankhla

Abstract Five species of tropical and warm temperate shrubs, bush morning glory (Ipomoea carnea N. von Jacquin subsp. fistulosa (K. von Martinus ex J. Choisy) D. Austin), Indian hawthorn (Raphiolepis indica (L.) J. Lindley), tropical hibiscus (Hibiscus rosa-sinensis L. ‘Brilliantissima’), jatropha (Jatropha integerrima N. von Jacquin), and nandina (Nandina domestica C.P. Thunberg), were grown in 2.8-liter (#1) black plastic containers at two contrasting nursery locations and regimes. In College Station, TX, plants were grown in full sun under high fertility conditions, while in Dallas, TX, plants were grown under 40% light exclusion and a lower fertility level. Plants at each location were sprayed to runoff, either once or twice, with a distilled water only control, a Latron B-1956 spreader sticker surfactant at 0.063 mg/liter (0.063 ppm) in distilled water, or cyclanilide [1-(2,4-dichlorophenyaminocarbonyl)-cyclopropane carboxylic acid] at 56, 112, or 223 mg/liter (56, 112, or 223 ppm, respectively) with the Latron surfactant in a distilled water carrier. Half of the plants in all treatments received a single application, while the other half received a second application two to three weeks later. Although growth responses and release of dormancy varied among species and with cyclanilide concentration, plants of most species had greater release of lateral buds from a dormant or quiescent state under the high irradiance and fertility conditions in College Station, compared to the lower irradiance and fertility conditions in Dallas. However, phytotoxicity symptoms as evidenced by lower quality ratings were also more prevalent in College Station. Phytotoxicity was moderate to severe on nearly all jatropha and tropical hibiscus plants exposed to cyclanilide. Toxicity symptoms and significant growth reductions were present on several species at 112 or 223 mg/liter (112 or 223 ppm, respectively). A second application usually increased the effects on growth responses at all concentrations and often induced phytotoxicity symptoms at 56 mg/liter (56 ppm). The disparate responses between the two locations suggest the importance of local growing conditions on the potential efficacy and predictability of responses to cyclanilide applications.


1991 ◽  
Vol 69 (2) ◽  
pp. 457-464 ◽  
Author(s):  
Dimitrios A. Stavroulakis ◽  
Nicolas Kalogerakis ◽  
Leo A. Behie ◽  
Kostas Iatrou

1971 ◽  
Vol 49 (7) ◽  
pp. 1253-1254 ◽  
Author(s):  
R. Latta

Development of a method of preserving suspension cultures of plant cells has been undertaken. When grown in a conventional medium containing 20 g/1 of sucrose, Daucus carota cells survived freezing and a short period of storage at −40 °C or −196 °C in the presence of a suitable protective agent, whereas Ipomoea sp. cells did not. Ipomoea cells survived freezing if they were adapted to growth in a medium containing 65 g/1 of sucrose.


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